Concept information
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Disorder of cellular component of blood (disorder)
anemia
Hemolytic anemia
Hereditary hemolytic anemia
...
Disorder of cellular component of blood (disorder)
anemia
Hemolytic anemia
Hereditary hemolytic anemia
...
Disorder of cellular component of blood (disorder)
Hemolytic disorder
Hemolytic anemia
Hereditary hemolytic anemia
Preferred term
Hereditary nonspherocytic haemolytic anaemia
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism
- HNSHA due to decreased adenosine deaminase activity
- HNSHA due to diphosphoglycerate mutase deficiency
- HNSHA due to gamma glutamyl cysteine synthetase deficiency
- HNSHA due to glucose phosphate isomerase deficiency
- HNSHA due to glutathione reductase deficiency
- HNSHA due to hexokinase deficiency
- HNSHA due to increased adenosine deaminase activity
- HNSHA due to NADH diaphorase deficiency
- HNSHA due to phophoglycerate kinase deficiency
- HNSHA due to phosphofructokinase deficiency
- HNSHA due to pyrimidine-5'-nucleotidase deficiency
- HNSHA due to pyruvate kinase deficiency
- HNSHA due to triosephosphate isomerase deficiency
Finding site
Has interpretation
Interprets
In other languages
URI
http://www.irandoc.acir/onto/irandoc/301317008
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